Investigations

1st investigations to order

karyotype

Test
Result
Test

Abnormalities include non-mosaic 45,X; mosaic 45,X (proportion of cells with a normal chromosome constitution); and fragmented X or Y (Xp deletions, isoXq chromosomes, Xq deletions, and ring X or Y chromosomes with substantial interstitial deletions).

A minimum of 20 cells need to be scored for chromosome number. The analysis is complete if mosaicism is confirmed. If one cell with a sex chromosome loss, gain or rearrangement is observed within the first 20 cells analysed, a minimum of 10 additional cells should be evaluated.

The test identifies 10% mosaicism or greater with 95% confidence.[5][28][29]

In patients with a strong suspicion of the diagnosis, if the test proves <10% of cells to be abnormal, more metaphases need to be counted along with fluorescence in situ hybridisation (FISH), or other cell types may be analysed with interphase FISH, in consultation with a geneticist/cytogeneticist.[30]

Result

at least 10% of the cells with a complete or partial loss of a sex chromosome

Investigations to consider

audiology testing

Test
Result
Test

Should be performed at the time of diagnosis and reassessed every 3-5 years.

Result

may be abnormal

ophthalmological examination

Test
Result
Test

Girls with Turner Syndrome have an epicanthal fold (upper eyelid fold that covers inner corner of eye) and hypertelorism (increased distance between eyes). A comprehensive ophthalmological examination should be performed between aged 12 and 18 months or at the time of diagnosis, if at an older age, to evaluate for refractive errors and other vision issues.

Result

Strabismus, amblyopia, hyperopia and myopia, ptosis and colour blindness have all been reported

bone age

Test
Result
Test

Radiography is the method of assessing skeletal maturation. Done on a pre-pubertal girl to assess potential for growth.

Result

mild delay; typically 2 years less than chronological age

echocardiogram

Test
Result
Test

Coarctation of the aorta may present in the neonatal period with cardiac failure or with hypertension. Bicuspid aortic valve occurs in approximately 30% of patients.

Routine trans-thoracic echocardiography may not obtain adequate visualisation of aortic valve, thoracic aorta, and pulmonary veins except, perhaps, in newborns.

Result

bicuspid aortic valve; coarctation of the aorta; dilated aorta; partial anomalous pulmonary veins; left heart hypoplasia

cardiac MRI

Test
Result
Test

Cardiac MR (CMR) is more effective than echocardiography and allows excellent visualisation of the entire thoracic aorta and great vessels, including pulmonary veins. [Figure caption and citation for the preceding image starts]: Cardiac MRI revealing normal aortic arch in ‘candy cane’ configuration on the left, compared with a previously undiagnosed aortic coarctation, just after the origin of the left subclavian artery (arrow), detected by MRI in an adult woman with Turner syndrome with severe upper body hypertensionFrom the personal collection of Carolyn Bondy, MS, MD (NIH study) [Citation ends].com.bmj.content.model.Caption@31ad0343

However, it requires sedation in the youngest patients and, thus, if clinical and echocardiographic evaluations appear normal, it is reasonable to wait until the girl is old enough to cooperate without sedation (usually 9-10 years).

Result

bicuspid aortic valve; coarctation of the aorta; dilated aorta; partial anomalous pulmonary veins; left heart hypoplasia

serum follicle-stimulating hormone and anti-Müllerian hormone

Test
Result
Test

An elevated follicle-stimulating hormone (FSH) and/or reduced anti-Müllerian hormone (AMH) predicts complete ovarian failure. However, ovarian potential cannot be predicted with certainty in young girls, as FSH levels elevate into the menopausal range at the age of normal puberty in those with ovarian failure.

Result

FSH-(abnormally) high; AMH-(abnormally) low

skeletal survey

Test
Result
Test

Performed in childhood at 5-6 years and 12-14 years to evaluate associated anomalies, such as wrist deformities and scoliosis.[5]

Madelung deformity (prominent distal ulna) is found in only about 5% of patients, but lesser degrees of wrist anomalies that can lead to functional problems are common.

Result

wrist deformities and scoliosis

pelvic ultrasound

Test
Result
Test

Performed in older girls and women.

The ovaries form normally in 45,X female fetuses, although most demonstrate accelerated oocyte death and ovarian degeneration into fibrous streaks.[21]

Result

immature uterus and streak ovaries

renal ultrasound

Test
Result
Test

Renal structural abnormalities affect approximately 25% of patients with Turner syndrome.[3][4]​​​

Renal function is usually normal, but obstruction of the collecting system is associated with urinary infection and may need correction.

Result

horseshoe or single kidney, or duplicated collecting system

thyroid function tests

Test
Result
Test

Performed in all patients at diagnosis.

Autoimmune thyroid disease (Hashimoto's thyroiditis and, less commonly, Graves' disease) is a common complication in Turner syndrome. These should be repeated annually.

Result

hypothyroidism or hyperthyroidism

antithyroid antibodies

Test
Result
Test

Autoimmune thyroid disease (Hashimoto's thyroiditis and, less commonly, Graves' disease) is a common complication in Turner syndrome.

Result

positive

LFTs/gamma glutamyl transferase/alkaline phosphatase

Test
Result
Test

About 30% to 40% of patients develop a complication of 'Turner hepatitis'. These should be tested after the age of 10 years and repeated annually.

Result

elevated AST, ALT, gamma glutamyl transferase

fasting glucose and HbA1c

Test
Result
Test

Diabetes is a common complication in Turner syndrome. Annual screening for diabetes risk includes fasting glucose and HbA1c. These should be tested after the age of 10 years and repeated annually.

Result

elevated

serum lipids

Test
Result
Test

Dyslipidaemia is common in Turner syndrome. These should be tested if aged 18 years or older, and if there is at least one risk factor for cardiovascular disease (check also regional recommendations).

Result

elevated

IgA level and tissue transglutaminase IgA

Test
Result
Test

Coeliac disease is common in Turner syndrome. These should be tested from aged 2 years and repeated every 2 years until adulthood, and then if symptomatic, repeated every 5 years.[5]

Result

elevated

vitamin D levels

Test
Result
Test

Vitamin D levels should be checked every 2-3 years after the age of 9 years until adulthood and every 3-5 years thereafter.[5]

Result

may be low

Use of this content is subject to our disclaimer